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Read our guarantee »Products:Signal Transduction >> Metabolism >> Energy Metabolism
Anti-Lactate Dehydrogenase antibody [EP1566Y]
See all Lactate Dehydrogenase products (10) ...
Rabbit monoclonal [EP1566Y] to Lactate Dehydrogenase
This antibody reacts with Lactate dehydrogenase
ICC/IF, WB, IP, Flow Cyt, IHC-Pmore details
Reacts with
Mouse, Rat, Human
Human liver carcinoma tissue and Hela cell lysate
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
pH: 7.40
Preservative: 0.01% Sodium azide
Constituents: 0.05% BSA, 40% Glycerol, 0.87% Sodium chloride, 0.09% Tris glycine
Tissue culture supernatant
Monoclonal
EP1566Y
IgG
Cancer >> Cancer Metabolism >> Metabolic signaling pathway >> Metabolism of carbohydrates
Cancer >> Tumor biomarkers >> Enzymes >> Lactic Dehydrogenase
Signal Transduction >> Metabolism >> Energy Metabolism
Our Abpromise guarantee covers the use of ab52488 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ICC/IF: 1/50 - 1/100.
WB: 1/100,000Detects a band of approximately 37 kDa (predicted molecular weight: 37 kDa).
IP: 1/100
Flow Cyt: 1/50 - 1/80.
IHC-P: 1/50 - 1/100.(It is strongly recommended to perform an antigen retrieval step for an enhanced signal.)
Lactate dehydrogenase (LDH) is present in a wide variety of organisms, including plants and animals. It is an oxidoreductase which catalyses the interconversion of pyruvate and lactate with concomitant interconversion of NADH and NAD+. As it can also catalyze the oxidation of hydroxybutyrate, it is occasionally called Hydroxybutyrate Dehydrogenase (HBD). There are 5 different isoenzymes of LDH, LDH1 to LDH5, each composed of 4 subunits which may be of 2 different types - M and H subunits. These subunits are encoded by two different genes: The M subunit is encoded by gene LDHA whilst the H subunit is encoded by LDHB. Usually LDH2 is the predominant form in the serum. An LDH1 level higher than the LDH2 level suggests myocardial infarction (damage to heart tissues releases heart LDH, which is rich in LDH1, into the bloodstream).
Cytoplasmic
Western blot - Lactate Dehydrogenase antibody [EP1566Y] (ab52488)
![Western blot - Lactate Dehydrogenase antibody [EP1566Y] (ab52488)](/ps/datasheet/Images/52/ab52488/ab52488_1.jpg)
Anti-Lactate Dehydrogenase antibody [EP1566Y] (ab52488) at 1/100000 dilution + Hela cell lysate at 10 µg
Secondary
Goat anti-rabbit HRP labeled at 1/2000 dilution
Predicted band size : 37 kDa
Observed band size : 37 kDa
Immunohistochemistry (Paraffin-embedded sections) - Lactate Dehydrogenase antibody [EP1566Y] (ab52488)
![Immunohistochemistry (Paraffin-embedded sections) - Lactate Dehydrogenase antibody [EP1566Y] (ab52488)](/ps/datasheet/Images/52/ab52488/ab52488_2.jpg)
Immunohistochemical analysis of paraffin-embedded human liver carcinoma using ab52488 at a 1/50 dilution.
Immunocytochemistry/ Immunofluorescence - Lactate Dehydrogenase antibody [EP1566Y] (ab52488)
![Immunocytochemistry/ Immunofluorescence - Lactate Dehydrogenase antibody [EP1566Y] (ab52488)](/ps/datasheet/images/52/ab52488/Lactate-Dehydrogenase-Primary-antibodies-ab52488-1.jpg)
ICC/IF image of ab52488 stained HeLa cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab52488, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
Flow Cytometry-Lactate Dehydrogenase antibody [EP1566Y](ab52488)
](/ps/datasheet/images/52/ab52488/Lactate-Dehydrogenase-Primary-antibodies-ab52488-2.jpg)
Overlay histogram showing HeLa cells stained with ab52488 (red line). The cells were fixed with methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab52488, 1/50 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (ab96899) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit monoclonal IgG (1µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a slightly decreased signal in HeLa cells fixed with 4% paraformaldehyde (10 min)/permeabilized in 0.1% PBS-Tween used under the same conditions.
This product has been referenced in:
See all 4 publications for this product
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![Western blot - Lactate Dehydrogenase antibody [EP1566Y] (ab52488)](/ps/datasheet/Images/52/ab52488/ab52488_1.jpg)
Anti-Lactate Dehydrogenase antibody [EP1566Y] (ab52488) at 1/100000 dilution + Hela cell lysate at 10 µg
Secondary
Goat anti-rabbit HRP labeled at 1/2000 dilution
Predicted band size : 37 kDa
Observed band size : 37 kDa
![Immunohistochemistry (Paraffin-embedded sections) - Lactate Dehydrogenase antibody [EP1566Y] (ab52488)](/ps/datasheet/Images/52/ab52488/ab52488_2.jpg)
Immunohistochemical analysis of paraffin-embedded human liver carcinoma using ab52488 at a 1/50 dilution.
![Immunocytochemistry/ Immunofluorescence - Lactate Dehydrogenase antibody [EP1566Y] (ab52488)](/ps/datasheet/images/52/ab52488/Lactate-Dehydrogenase-Primary-antibodies-ab52488-1.jpg)
ICC/IF image of ab52488 stained HeLa cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab52488, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
](/ps/datasheet/images/52/ab52488/Lactate-Dehydrogenase-Primary-antibodies-ab52488-2.jpg)
Overlay histogram showing HeLa cells stained with ab52488 (red line). The cells were fixed with methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab52488, 1/50 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (
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